David Zuniga Avalos
⚠️ Moderate Risk
FEI: 3004690599 • Cihuatlan, Jalisco • MEXICO
FEI Number
3004690599
Location
Cihuatlan, Jalisco
Country
MEXICOAddress
Manuel Garcia Mes # 128, , Cihuatlan, Jalisco, Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
Frequently Asked Questions
What is David Zuniga Avalos's FDA import refusal history?
David Zuniga Avalos (FEI: 3004690599) has 2 FDA import refusal record(s) in our database, spanning from 4/18/2007 to 9/5/2007.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. David Zuniga Avalos's FEI number is 3004690599.
What types of violations has David Zuniga Avalos received?
David Zuniga Avalos has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about David Zuniga Avalos come from?
All FDA import refusal data for David Zuniga Avalos is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.